Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Alcat Test


Nancy W

Recommended Posts

Nancy W Newbie

Has anyone heard of this blood test? It is for food sensitivities. I have been diagnosed as celiac for less than one year. I had this test done and it said that I am sensitive to whey, chicken, turkey, peanuts, soy, yeast, vinegar, rice, and not to mention coffee, lettuce, corn, squash, etc. I'm not supposed to eat these foods for three to six months, and after that period, I can reintroduce the foods on a rotation diet. You can imagine how miserable this has made me when I already can't have gluten. Oddly enough, the test said that I have no reaction to gluten. I suppose because it tests for sensitivities, not allergies. I have decided to just eat a normal gluten-free diet because otherwise, I'll starve! I was wondering if anyone has any opinion on this?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Rachel--24 Collaborator

I'm not familiar with the test but do the foods that came up positive actually bother you? I would eliminate some of the foods you might suspect you are sensitive to and then after a few weeks add one back in...eat it for a few days and if you get symptoms you know to avoid it. Do this with each food. Make sure you are feeling pretty good before you add a new food.

Also Celiac is not an allergy so gluten wont show up in an allergy test or a sensitivity test. Its an autoimmune reaction...far different from an allergy.

Claire Collaborator

I am not familiar with this test but certainly am well acquainted with food sensitivity testing. Be aware that as good as these tests can be, they produce a lot of false positives. Where you have been given so many 'reactives' you need to pick out the ones that you are quite sure don't bother you and put them to the test.

Remove from the diet for at least two weeks - then reintroduce - beginning in the early morning. When you do this try to keep any of the other reactives on the list out of the diet. Eat the reintroduced food liberally. If there is no detectable reaction, consider the food safe and after a few days - test another. If you get a reaction, don't test any other food for another couple of weeks. Claire

ravenwoodglass Mentor
Has anyone heard of this blood test? It is for food sensitivities. I have been diagnosed as celiac for less than one year. I had this test done and it said that I am sensitive to whey, chicken, turkey, peanuts, soy, yeast, vinegar, rice, and not to mention coffee, lettuce, corn, squash, etc. I'm not supposed to eat these foods for three to six months, and after that period, I can reintroduce the foods on a rotation diet. You can imagine how miserable this has made me when I already can't have gluten. Oddly enough, the test said that I have no reaction to gluten. I suppose because it tests for sensitivities, not allergies. I have decided to just eat a normal gluten-free diet because otherwise, I'll starve! I was wondering if anyone has any opinion on this?

Just as an aside, I had allergy testing done before going gluten-free and was allergic to everything. This was because my immune system was in overdrive. Many sensitivities went away after I healed.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,688
    • Most Online (within 30 mins)
      7,748

    Princess.dfc
    Newest Member
    Princess.dfc
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Yes, some people with Celiac do react to quinoa.  I know i do.  Apparently, two different "breeds" of quinoa can stimulate the immune system. Read here... Variable activation of immune response by quinoa (Chenopodium quinoa Willd.) prolamins in celiac disease https://pubmed.ncbi.nlm.nih.gov/22760575/#:~:text=Cultivars Ayacuchana and Pasankalla stimulated,for patients with celiac disease. And some of us react to corn (maize) as well. Maize prolamins could induce a gluten-like cellular immune response in some celiac disease patients https://pubmed.ncbi.nlm.nih.gov/24152750/   P.S. @Brook G have you thought about getting a genetic test done for known Celiac genes?  
    • Brook G
      People who are Celiac don't have a gluten response to Quinoa, but some people who are gluten intolerant do.  I react to quinoa just like I do to gluten.  Freddies/Kroger came out with their own gluten-free Bread and I didn't think to read the ingredients.  I couldn't figure out where I would have gotten gluten in my diet until I read the ingredients in their bread... QUINOA
    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
×
×
  • Create New...